LDH info

Canonical Allele Identifier: CA233479800
Gene: SLCO1B3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17680137

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20862972C>G , CM000674.2:g.20862972C>G GRCh38
NC_000012.11:g.21015906C>G , CM000674.1:g.21015906C>G GRCh37
NC_000012.10:g.20907173C>G NCBI36
NG_032071.1:g.57269C>G

Transcript Alleles

HGVS Amino-acid change
NM_019844.3:c.727+118C>G VV NP_062818.1:p.=
NM_001349920.1:c.643+118C>G VV NP_001336849.1:p.=
NM_001349920.2:c.643+118C>G VV NP_001336849.1:p.=
NM_001371097.1:c.727+118C>G VV NP_001358026.1:p.=
NM_019844.4:c.727+118C>G VV MANE Preferred NP_062818.1:p.=
ENST00000261196.6:c.727+118C>G ENSP00000261196.2:p.=
ENST00000381541.7:c.359+4401C>G ENSP00000370952.3:p.=
ENST00000381545.7:c.727+118C>G ENSP00000370956.3:p.=
ENST00000540229.1:c.727+118C>G ENSP00000441269.1:p.=
ENST00000540853.5:c.727+118C>G ENSP00000442000.1:p.=
ENST00000544370.1:n.199+118C>G ENSP00000443225.1:p.=